N2644
NωNitro-L-arginine benzyl ester p-toluenesulfonate salt
≥95% (TLC)
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About This Item
Empirical Formula (Hill Notation):
C13H19N5O4 · C7H8O3S
CAS Number:
Molecular Weight:
481.52
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
assay
≥95% (TLC)
application(s)
peptide synthesis
storage temp.
−20°C
SMILES string
Cc1ccc(cc1)S(O)(=O)=O.N[C@@H](CCCNC(=N)N[N+]([O-])=O)C(=O)OCc2ccccc2
InChI
1S/C13H19N5O4.C7H8O3S/c14-11(7-4-8-16-13(15)17-18(20)21)12(19)22-9-10-5-2-1-3-6-10;1-6-2-4-7(5-3-6)11(8,9)10/h1-3,5-6,11H,4,7-9,14H2,(H3,15,16,17);2-5H,1H3,(H,8,9,10)/t11-;/m0./s1
InChI key
DUIFZPVSNBDNLZ-MERQFXBCSA-N
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D Y Cheng et al.
The American journal of physiology, 266(6 Pt 2), H2416-H2422 (1994-06-01)
The comparative effects of the nitric oxide (NO) synthase inhibitors N omega-nitro-L-arginine (L-NNA), N omega-nitro-L-arginine methyl ester (L-NAME), and N omega-nitro-L-arginine benzyl ester (L-NABE) on baseline tone and on vasodilator responses to acetylcholine (ACh), bradykinin (BK), and substance P (SP)
B J DeWitt et al.
The American journal of physiology, 273(3 Pt 1), L588-L594 (1997-10-08)
The effects of the nitric oxide (NO) synthesis inhibitor L-N5-(1-iminoethyl)-ornithine (L-NIO) on baseline tone and on responses to the endothelium-dependent vasodilator agents were investigated in the pulmonary vascular bed of the cat under constant-flow conditions. When administered in doses of
J Wayte et al.
Neuroreport, 8(1), 267-271 (1996-12-20)
[3H]L-arginine uptake and the conversion of [3H]L-arginine to [3H]citrulline were characterized in foetal hypothalamic cultures. [3H]L-arginine uptake was reduced by L-ornithine (10 microM-1 mM), high extracellular K+ (56 mM), L-glutamate (100 microM) and removal of extracellular Ca2+, but was increased